Canonical Allele Identifier: PA2826376576
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 703249
ClinVar RCV Id: RCV000872747 RCV001549674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Met2601Leu
CA8241014
NM_001256183.2:c.7801A>C
CA397146330
NM_001256183.2:c.7801A>T